The Clinical and Biochemical Spectrum of Congenital Adrenal Hyperplasia Secondary to 21-Hydroxylase Deficiency

21-Hydroxylase Deficiency (21-OH Deficiency) represents the most common form of Congenital Adrenal Hyperplasia (CAH), a complex and heterogenous group of conditions, characterised by defects in one of the five enzymes involved in adrenal steroidogenesis. Defects in this steroidogenic enzyme, the pro...

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Autores principales: Huynh, Tony, McGown, Ivan, Cowley, David, Nyunt, Ohn, Leong, Gary M, Harris, Mark, Cotterill, Andrew M
Formato: Artigo
Lenguaje:Inglês
Publicado: The Australian Association of Clinical Biochemists 2009
Materias:
Review Article
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC2702216/
https://ncbi.nlm.nih.gov/pubmed/19565027
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